All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06239 CIMAH Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia 617780 AR 0 0 MTHFD1 - -
02381 NTDFS neural tube defects, folate-sensitive (NTDFS) 601634 AR 0 0 MTHFD1, MTHFR, MTR, MTRR - -
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